反应 #1885047

反应方程式

NaHCO3

chlorosulfonic acid

(3R,3′S)-3-(3,5-dichlorophenyl)-1′-phenyl-1,3′-bipyrrolidin-2′-one

chlorosulfonic acid

→

4-[(3R,3′S)-3-(3,5-dichlorophenyl)-2′-oxo-1,3′-bipyrrolidin-1′-yl]benzene-1-sulfonyl chloride

收率 88.0%

溶剂

DCE

反应条件

后处理

1. 1
   其他Synthesized
2. 2
   workup.STIRRINGthe reaction mixture was stirred at 50° C. for 1 hour
3. 3
   温度the reaction mixture was then heated to 70° C. for 10 min
4. 4
   温度cooled to RT
5. 5
   workup.ADDITIONslowly poured onto ice water
6. 6
   萃取the reaction mixture was extracted with EtOAc (3×)
7. 7
   洗涤The combined organic phases were washed with water, brine
8. 8
   干燥dried over MgSO4
9. 9
   其他evaporated to dryness

实验过程

Synthesized according to General Procedure 11. To a solution of (3R,3′S)-3-(3,5-dichlorophenyl)-1′-phenyl-1,3′-bipyrrolidin-2′-one (900 mg, 2.40 mmol) in DCE (10 mL) at 0° C. was added chlorosulfonic acid (1.40 g, 800 μL, 12.0 mmol) slowly. The reaction mixture was then stirred at 0° C. for 30 min, at RT for 1 hour and at 50° C. for 1 hour. At this time more chlorosulfonic acid (279 mg, 160 μL, 2.40 mmol) was added and the reaction mixture was stirred at 50° C. for 1 hour, the reaction mixture was then heated to 70° C. for 10 min, cooled to RT and slowly poured onto ice water. The pH was brought to ˜7 with saturated aqueous NaHCO3 and the reaction mixture was extracted with EtOAc (3×). The combined organic phases were washed with water, brine, dried over MgSO4 and evaporated to dryness to afford 4-[(3R,3′S)-3-(3,5-dichlorophenyl)-2′-oxo-1,3′-bipyrrolidin-1′-yl]benzene-1-sulfonyl chloride as a tan solid (1.00 g, 88%). LC/MS (10%-99% CH3CN (0.035% TFA)/H2O (0.05% TFA)), m/z: M+1 obs=473.3; tR=1.58 min.

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